P2X7 receptors and pannexin1 hemichannels shape presynaptic transmission.

IF 3 4区 医学 Q2 NEUROSCIENCES Purinergic Signalling Pub Date : 2024-06-01 Epub Date: 2023-09-15 DOI:10.1007/s11302-023-09965-8
Nathalia Vitureira, Alberto Rafael, Verónica Abudara
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Abstract

Over the last decades, since the discovery of ATP as a transmitter, accumulating evidence has been reported about the role of this nucleotide and purinergic receptors, in particular P2X7 receptors, in the modulation of synaptic strength and plasticity. Purinergic signaling has emerged as a crucial player in orchestrating the molecular interaction between the components of the tripartite synapse, and much progress has been made in how this neuron-glia interaction impacts neuronal physiology under basal and pathological conditions. On the other hand, pannexin1 hemichannels, which are functionally linked to P2X7 receptors, have appeared more recently as important modulators of excitatory synaptic function and plasticity under diverse contexts. In this review, we will discuss the contribution of ATP, P2X7 receptors, and pannexin hemichannels to the modulation of presynaptic strength and its impact on motor function, sensory processing, synaptic plasticity, and neuroglial communication, with special focus on the P2X7 receptor/pannexin hemichannel interplay. We also address major hypotheses about the role of this interaction in physiological and pathological circumstances.

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P2X7 受体和 pannexin1 半通道形成突触前传导
自发现 ATP 作为一种递质以来的几十年间,有关这种核苷酸和嘌呤能受体(尤其是 P2X7 受体)在调节突触强度和可塑性方面的作用的证据不断积累。嘌呤能信号已成为协调三方突触各组成部分之间分子相互作用的关键角色,在这种神经元-胶质细胞相互作用如何影响神经元在基础和病理条件下的生理学方面已取得了很大进展。另一方面,在功能上与 P2X7 受体相关联的 pannexin1 半通道最近作为兴奋性突触功能和可塑性的重要调节剂出现在各种情况下。在这篇综述中,我们将讨论 ATP、P2X7 受体和 pannexin 半通道对突触前强度调节的贡献及其对运动功能、感觉处理、突触可塑性和神经胶质沟通的影响,并特别关注 P2X7 受体/pannexin 半通道的相互作用。我们还探讨了有关这种相互作用在生理和病理情况下的作用的主要假设。
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来源期刊
Purinergic Signalling
Purinergic Signalling 医学-神经科学
CiteScore
6.60
自引率
17.10%
发文量
75
审稿时长
6-12 weeks
期刊介绍: Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the established neurotransmitters in both peripheral and central nervous systems. Four subtypes of P1 (adenosine) receptors, 7 subtypes of P2X ion channel receptors and 8 subtypes of P2Y G protein-coupled receptors have currently been identified. Since P2 receptors were first cloned in the early 1990’s, there is clear evidence for the widespread distribution of both P1 and P2 receptor subtypes in neuronal and non-neuronal cells, including glial, immune, bone, muscle, endothelial, epithelial and endocrine cells.
期刊最新文献
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